Exp Mol Med.  2000 Dec;32(4):231-234.

Y chromosome microdeletions in idiopathic azoospermia and non-mosaic type of Klinefelter syndrome

Affiliations
  • 1Department of Obstetrics and Gynecology, College of Medicine, Korea University Anam Hospital, Seoul.

Abstract

The objective of this study was to elucidate the cause of the spermatogenic defect in idiopathic azoospermia and non-mosaic type of Klinefelter syndrome. Genomic DNAs from 9 cases of Korean idiopathic azoospermia and 6 of Korean non-mosaic type of Klinefelter syndrome were used for the detection of Y chromosome microdeletions by polymerase chain reaction using 60 primers. Microdeletions of the Y chromosome were found in 1 of 9 (11.1%) patients with idiopathic azoospermia, whereas none was deleted in non-mosaic type of Klinefelter syndrome. This result suggests that Y chromosome microdeletions could be one of the etiologic factors in idiopathic azoospermia.

Keyword

Y chromosome; microdeletion; idiopathic azoospermia; Klinefelter syndrome

MeSH Terms

Gene Dosage
Human
Klinefelter Syndrome/classification/*genetics
Male
Oligospermia/classification/*genetics
Polymerase Chain Reaction
*Sequence Deletion
Sequence Tagged Sites
Spermatogenesis
X Chromosome/genetics
Y Chromosome/*genetics
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